Canonical Allele Identifier: CA1226667773
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs1663372126

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230705941_230705942insCCTACCGGGGAGAC , CM000663.2:g.230705941_230705942insCCTACCGGGGAGAC GRCh38
NC_000001.10:g.230841687_230841688insCCTACCGGGGAGAC , CM000663.1:g.230841687_230841688insCCTACCGGGGAGAC GRCh37
NC_000001.9:g.228908310_228908311insCCTACCGGGGAGAC NCBI36
NG_008836.1:g.13649_13650insGTCTCCCCGGTAGG
NG_008836.2:g.13649_13650insGTCTCCCCGGTAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1088_1089insGTCTCCCCGGTAGG MANE Select ENSP00000355627.5:p.Thr367Ter
ENST00000679684.1:c.1088_1089insGTCTCCCCGGTAGG ENSP00000505981.1:p.Thr367Ter
ENST00000679738.1:c.1088_1089insGTCTCCCCGGTAGG ENSP00000505063.1:p.Thr367Ter
ENST00000679802.1:c.*547_*548insGTCTCCCCGGTAGG ENSP00000505184.1:p.=
ENST00000679854.1:n.5393_5394insGTCTCCCCGGTAGG
ENST00000679957.1:c.1088_1089insGTCTCCCCGGTAGG ENSP00000506646.1:p.Thr367Ter
ENST00000680041.1:c.1088_1089insGTCTCCCCGGTAGG ENSP00000504866.1:p.Thr367Ter
ENST00000680783.1:c.829+4053_829+4054insGTCTCCCCGGTAGG ENSP00000506329.1:p.=
ENST00000681269.1:c.1088_1089insGTCTCCCCGGTAGG ENSP00000505985.1:p.Thr367Ter
ENST00000681347.1:n.1599_1600insGTCTCCCCGGTAGG
ENST00000681514.1:c.1088_1089insGTCTCCCCGGTAGG ENSP00000505963.1:p.Thr367Ter
ENST00000681772.1:c.1088_1089insGTCTCCCCGGTAGG ENSP00000505829.1:p.Leu363=
ENST00000366667.4:c.1115_1116insGTCTCCCCGGTAGG ENSP00000355627.4:p.Thr376Ter
NM_000029.3:c.1115_1116insGTCTCCCCGGTAGG NP_000020.1:p.Thr376Ter
NM_000029.4:c.1115_1116insGTCTCCCCGGTAGG NP_000020.1:p.Thr376Ter
NM_001382817.3:c.1088_1089insGTCTCCCCGGTAGG NP_001369746.2:p.Thr367Ter
NM_001384479.1:c.1088_1089insGTCTCCCCGGTAGG MANE Select NP_001371408.1:p.Thr367Ter